Canonical Allele Identifier: CA499890727

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143300495
• MyVariant Identifiers: chr17:g.37884072C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727819C>T , CM000679.2:g.39727819C>T	GRCh38
NC_000017.10:g.37884072C>T , CM000679.1:g.37884072C>T	GRCh37
NC_000017.9:g.35137598C>T	NCBI36
NG_007503.1:g.44680C>T , LRG_724:g.44680C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3543C>T MANE Select	ENSP00000269571.4:p.Val1181=
ENST00000269571.9:c.3543C>T	ENSP00000269571.4:p.Val1181=
ENST00000406381.6:c.3453C>T	ENSP00000385185.2:p.Val1151=
ENST00000445658.6:c.2715C>T	ENSP00000404047.2:p.Val905=
ENST00000541774.5:c.3498C>T	ENSP00000446466.1:p.Val1166=
ENST00000578373.5:c.*3333C>T	ENSP00000463427.1:n.*3333C>T
ENST00000584450.5:c.*122C>T	ENSP00000463714.1:n.*122C>T
ENST00000584601.5:c.3453C>T	ENSP00000462438.1:p.Val1151=
NM_001005862.2:c.3453C>T , LRG_724t1:c.3453C>T	NP_001005862.1:p.Val1151=
NM_001289936.1:c.3498C>T , LRG_724t4:c.3498C>T	NP_001276865.1:p.Val1166=
NM_001289937.1:c.*122C>T	NP_001276866.1:n.*122C>T
NM_004448.3:c.3543C>T , LRG_724t2:c.3543C>T	NP_004439.2:p.Val1181=
NR_110535.1:n.3867C>T
XM_024450641.1:c.3681C>T	XP_024306409.1:p.Val1227=
XM_024450642.1:c.3636C>T	XP_024306410.1:p.Val1212=
XM_024450643.1:c.3591C>T	XP_024306411.1:p.Val1197=
NM_001005862.3:c.3453C>T	NP_001005862.1:p.Val1151=
NM_001289936.2:c.3498C>T	NP_001276865.1:p.Val1166=
NM_001289937.2:c.*122C>T	NP_001276866.1:n.*122C>T
NM_001382782.1:c.3453C>T	NP_001369711.1:p.Val1151=
NM_001382783.1:c.3453C>T	NP_001369712.1:p.Val1151=
NM_001382784.1:c.3660C>T	NP_001369713.1:p.Val1220=
NM_001382785.1:c.3645C>T	NP_001369714.1:p.Val1215=
NM_001382786.1:c.3624C>T	NP_001369715.1:p.Val1208=
NM_001382787.1:c.3618C>T	NP_001369716.1:p.Val1206=
NM_001382788.1:c.3573C>T	NP_001369717.1:p.Val1191=
NM_001382789.1:c.3564C>T	NP_001369718.1:p.Val1188=
NM_001382790.1:c.3540C>T	NP_001369719.1:p.Val1180=
NM_001382791.1:c.3534C>T	NP_001369720.1:p.Val1178=
NM_001382792.1:c.3507C>T	NP_001369721.1:p.Val1169=
NM_001382793.1:c.3501C>T	NP_001369722.1:p.Val1167=
NM_001382794.1:c.3501C>T	NP_001369723.1:p.Val1167=
NM_001382795.1:c.3495C>T	NP_001369724.1:p.Val1165=
NM_001382796.1:c.3456C>T	NP_001369725.1:p.Val1152=
NM_001382797.1:c.3444C>T	NP_001369726.1:p.Val1148=
NM_001382798.1:c.3387C>T	NP_001369727.1:p.Val1129=
NM_001382799.1:c.3363C>T	NP_001369728.1:p.Val1121=
NM_001382800.1:c.3357C>T	NP_001369729.1:p.Val1119=
NM_001382801.1:c.3339C>T	NP_001369730.1:p.Val1113=
NM_001382802.1:c.3285C>T	NP_001369731.1:p.Val1095=
NM_001382803.1:c.*122C>T	NP_001369732.1:n.*122C>T
NM_001382804.1:c.2715C>T	NP_001369733.1:p.Val905=
NM_001382805.1:c.2592C>T	NP_001369734.1:p.Val864=
NM_001382806.1:c.2505C>T	NP_001369735.1:p.Val835=
NM_004448.4:c.3543C>T MANE Select	NP_004439.2:p.Val1181=
NR_110535.2:n.3781C>T